US2461551A - Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal - Google Patents
Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal Download PDFInfo
- Publication number
- US2461551A US2461551A US640676A US64067646A US2461551A US 2461551 A US2461551 A US 2461551A US 640676 A US640676 A US 640676A US 64067646 A US64067646 A US 64067646A US 2461551 A US2461551 A US 2461551A
- Authority
- US
- United States
- Prior art keywords
- styrene
- coal
- butadiene
- resin
- copolymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229920001577 copolymer Polymers 0.000 title description 42
- 239000011347 resin Substances 0.000 title description 29
- 229920005989 resin Polymers 0.000 title description 29
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title description 26
- 239000003245 coal Substances 0.000 title description 23
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 title description 16
- 239000000203 mixture Substances 0.000 title description 8
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 238000003801 milling Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000013329 compounding Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- 239000004853 Utah resin Substances 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- BECGPAPCGOJSOT-UHFFFAOYSA-N [O-2].O.S.[Zn+2] Chemical compound [O-2].O.S.[Zn+2] BECGPAPCGOJSOT-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 238000010057 rubber processing Methods 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L57/00—Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C08L57/02—Copolymers of mineral oil hydrocarbons
Definitions
- butadiene-styrene rubbery copolymers such as GR-S, Buna S, and the like have gone into extensive use during the past few years, the processing of this type of synthetic rubber presents various difiiculties which render the working thereof prolonged and expensive.
- butadiene-styrene rubbery copolymers of this type exhibit a decided lack of tack or cohesive bonding, which weakness leads to difiiculty in the handling of such copolymers on conventional rubber-working machinery, especially the customary roll mill.
- This difficulty in handling evidences itself principally in poor following of the rolls of a roll mill and in poor acceptance or wetting of reinforcing fillers and pigments by such rubbery copolymers.
- butadiene-styrene rubbery copolymers can be materially improved by incorporating therewith a small amount of a Utah-type coal resin.
- the presence of the coal resin has been found to reduce the time and the cost of milling a butadiene-styrene copolymer and of incorporating compoundin ingredients therewith.
- the addition of the coal resin serves to increase the tack of butadiene-styrene copolymers containing from about 20% to about 30% styrene to such an extent that the proces'sability thereof is brought substantially to a par with that of natural rubber.
- Such a butadiene-styrene rubbery copolymer containing a Utah-type coal resin not only follows rolls properly but also readily accepts the necessary amounts of pigments, fillers, and the like customarily added to rubbery materials during the processing thereof. Moreover, the presence of the Utah-type coal resin does not adversely aiiect the curing of the milled butadiene-styrene rubbery compound, and the cured compounded copolymer exhibits good tensile strength, ultimate elongat on, and hardness.
- the coal resin which we incorporate with butadiene-styrene copolymers is obtained from resinbearing coals such as those found in extensive deposits in Utah. These coals, particularly those obtained from the Utah deposits, contain substantial percentages (up to 5% and more) of such resinous material, which maybe separated and recovered therefrom in various manners.
- the resin is preferably employed in a coal-free condition. It can advantageously be recovered from the coal by the following two-stage procedure:
- the resin is first separated from the bulk of the coal by aqueous flotation as described, for example, in Green, 1,773,997.
- the resulting resin concentrate which still contains an appreciable proportion of coal (up to 15 to 20%) admixed therewith, is then dissolved in a solvent composed essentially of saturated hydrocarbons having 6 or less carbon atoms in accordance with the disclosure of the copending Lee application, Serial No. 515,804, filed December 27, 1943, now abandoned.
- the insoluble coal is separated from the resultin resin solution by filtration, and the resin itself is then recovered in a substantially coal-free'condition by vaporization of the solvent from the solution. If a light-colored resin product is desired, the resin solution may be filtered through a bed of activated clay or the like.
- a typical Utah-type coal resin, recovered in this manner, is soluble in ethers, petroleum and coal-tar hydrocarbons, and vegetable oils, partially soluble in esters and ketones, and insoluble in the lower alcohols.
- the following physical and chemical characteristics are typical of a representative Utah-type coal resin which has been recovered by extraction with hexane:
- the coal resin is advantageously compounded with a butadiene-styrene rubbery copolymer, 'especially a copolymer containing from about 20% to about 30% styrene, in an amount ranging from about. 5 to about 25% based on the weightof the copolymer. Within this range of proportions occurs the most significant increase in processibility of the rubbery copolymer with the pro- 3 duction of a cured product having the most desirable characteristics. Less than 5% of the coal resin may be used, but in such case the increase in processibility of the copolymer may not be sufficient to permit the ready incorporation therewith of the desired amounts of pigments and fillers. More than 25% of the coal resin may also be employed.
- Suilicient coal resin should, of course, be incorporated with the butadiene-styrene copolymer to improve its processing characteristics and to enable it to be broken down on milling to the extent necessary for the desired purpose.
- the resin may be incorporated with the copolymer either before the copolymer is passed through a roll mill or other rubber handling equipment or during the milling of the copolymer.
- GH rubber a copolymer of about 75% butadiene and 25% styrene compounded with a coal-free Utah-type coal resin:
- Example 1 A GR-S-containing tire-tread stock was prepared from the following materials:
- the presence of the coal resin rendered the milling of the GR-S copolymer and the incorporation of the other ingredients therewith much more easy.
- the milled copolymer compound possessed an increased dry tack and exhibited an excellent tack when it was washed with gasoline.
- Example 2 The following formulation illustrates a (33-8 copolymer compound having a very high degree of tackiness.
- the compoundedGR-S was readily millable.
- a composition comprising a rubbery copolymer of butadiene and styrene and 5-25% on the weight of the copolymer of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals.
- composition as claimed in claim 1 in which the rubbery copolymer of butadiene and styrene contains from about 20% to about 30% styrene.
- composition as claimed in claim 1 in which the rubbery copolymer of butadiene and styrene contains approximately butadiene and 25% styrene.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Description
Patented Feb. 15, 1949 COMPOSITION COMPRISING A RUBBERY CO- POLYMER OF BUTADIENE AND STYRENE AND A RESIN OCCURRING IN UTAH RESDI- BEARING COAL Ernest D. Lee, Teaneck, and Loy S. Engle, Harrington Park, N. J assignors to Interchemical Corporation, New York, N. Y., a corporation of Ohio No Drawing. Application January 11, 1946,
Serial No. 640,676
6 Claims. (01. 260- 27) diene-styrene rubbery copolymers and is particularly directed to the improvement of the processing characteristics thereof'whereby such copolymers can be more readily handled by the customary rubber-processing equipment. More especially, the present invention is concerned with the improvement of the tackiness of a butadiene-styrene rubbery copolymer containing from about to about 30% styrene.
Although butadiene-styrene rubbery copolymers such as GR-S, Buna S, and the like have gone into extensive use during the past few years, the processing of this type of synthetic rubber presents various difiiculties which render the working thereof prolonged and expensive. In particular, butadiene-styrene rubbery copolymers of this type exhibit a decided lack of tack or cohesive bonding, which weakness leads to difiiculty in the handling of such copolymers on conventional rubber-working machinery, especially the customary roll mill. This difficulty in handling evidences itself principally in poor following of the rolls of a roll mill and in poor acceptance or wetting of reinforcing fillers and pigments by such rubbery copolymers.
We have now found that the processing characteristics of butadiene-styrene rubbery copolymers can be materially improved by incorporating therewith a small amount of a Utah-type coal resin. The presence of the coal resin has been found to reduce the time and the cost of milling a butadiene-styrene copolymer and of incorporating compoundin ingredients therewith. In particular, the addition of the coal resin serves to increase the tack of butadiene-styrene copolymers containing from about 20% to about 30% styrene to such an extent that the proces'sability thereof is brought substantially to a par with that of natural rubber. Such a butadiene-styrene rubbery copolymer containing a Utah-type coal resin not only follows rolls properly but also readily accepts the necessary amounts of pigments, fillers, and the like customarily added to rubbery materials during the processing thereof. Moreover, the presence of the Utah-type coal resin does not adversely aiiect the curing of the milled butadiene-styrene rubbery compound, and the cured compounded copolymer exhibits good tensile strength, ultimate elongat on, and hardness. The
addition of the coal resin also effects a decided reduction in the nerve of the copolymer,
The coal resin which we incorporate with butadiene-styrene copolymers is obtained from resinbearing coals such as those found in extensive deposits in Utah. These coals, particularly those obtained from the Utah deposits, contain substantial percentages (up to 5% and more) of such resinous material, which maybe separated and recovered therefrom in various manners. In accordance with the present invention, the resin is preferably employed in a coal-free condition. It can advantageously be recovered from the coal by the following two-stage procedure:
The resin is first separated from the bulk of the coal by aqueous flotation as described, for example, in Green, 1,773,997. The resulting resin concentrate, which still contains an appreciable proportion of coal (up to 15 to 20%) admixed therewith, is then dissolved in a solvent composed essentially of saturated hydrocarbons having 6 or less carbon atoms in accordance with the disclosure of the copending Lee application, Serial No. 515,804, filed December 27, 1943, now abandoned. The insoluble coal is separated from the resultin resin solution by filtration, and the resin itself is then recovered in a substantially coal-free'condition by vaporization of the solvent from the solution. If a light-colored resin product is desired, the resin solution may be filtered through a bed of activated clay or the like.
A typical Utah-type coal resin, recovered in this manner, is soluble in ethers, petroleum and coal-tar hydrocarbons, and vegetable oils, partially soluble in esters and ketones, and insoluble in the lower alcohols. The following physical and chemical characteristics are typical of a representative Utah-type coal resin which has been recovered by extraction with hexane:
Specific gravity 1.03-1.06 Softening point (mercury method)- C. Melting point (mercury method) 180 C.
Refractive index 1.544 Physical state Brittle solid Acid value 6-8 Iodine number 100-140 Molecular weight (average) 1000 Analysis:
Carbon 86.95% Hydrogen 11.10% Oxygen 1.95%
The coal resin is advantageously compounded with a butadiene-styrene rubbery copolymer, 'especially a copolymer containing from about 20% to about 30% styrene, in an amount ranging from about. 5 to about 25% based on the weightof the copolymer. Within this range of proportions occurs the most significant increase in processibility of the rubbery copolymer with the pro- 3 duction of a cured product having the most desirable characteristics. Less than 5% of the coal resin may be used, but in such case the increase in processibility of the copolymer may not be sufficient to permit the ready incorporation therewith of the desired amounts of pigments and fillers. More than 25% of the coal resin may also be employed. but in such event the cured compounded copolymer may be too boardy for certain applications. Suilicient coal resin should, of course, be incorporated with the butadiene-styrene copolymer to improve its processing characteristics and to enable it to be broken down on milling to the extent necessary for the desired purpose. The resin may be incorporated with the copolymer either before the copolymer is passed through a roll mill or other rubber handling equipment or during the milling of the copolymer.
The following examples illustrate typical formulations of GH rubber (a copolymer of about 75% butadiene and 25% styrene) compounded with a coal-free Utah-type coal resin:
Example 1 A GR-S-containing tire-tread stock was prepared from the following materials:
Parts by weight GR-S 250 Carbon .black 135 Utah-type coal resin (coal-free) 45 Zinc oxide Sulfur 6 Condensation product of mercaptobenzothiazole with cyclohexylamine 5 .25
The presence of the coal resin rendered the milling of the GR-S copolymer and the incorporation of the other ingredients therewith much more easy. The milled copolymer compound possessed an increased dry tack and exhibited an excellent tack when it was washed with gasoline.
Example 2 The following formulation illustrates a (33-8 copolymer compound having a very high degree of tackiness.
The compoundedGR-S was readily millable.
. g 4 The coal resin imparted an extremely high degree oi. tack to the copolymer compound as evidenced by the fact that two pieces of the milled compound were self-sealing when placed together. Samples of the milled compound were cured for one hour at 350 F. and were found to have the following properties:
Tensile strength --lbs. per sq. inch 1860 Elongation (ultimate) --per cent 2800 Shore hardness per cent We claim:
1. A composition comprising a rubbery copolymer of butadiene and styrene and 5-25% on the weight of the copolymer of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals.
2. The composition as claimed in claim 1, in which the rubbery copolymer of butadiene and styrene contains from about 20% to about 30% styrene.
3. The composition as claimed in claim 1, in which the rubbery copolymer of butadiene and styrene contains approximately butadiene and 25% styrene.
4. In the method of compounding a butadienestyrene rubbery copolymer, the steps of incorporating with such a copolymer 5 to 25%, based on the weight of the copolymer, of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals, and milling the mixture to obtain a rubber compound.
5. The method of compounding a butadienestyrene rubbery copolymer as claimed in claim 4 in which the rubbery copolymer contains from about 20% to about 30% styrene.
6. The method of compounding a butadienestyrene rubbery copolymer as claimed in claim 4 in which the rubbery copolymer contains approximately 75% butadiene and 25% styrene.
ERNEST D. LEE. LOY S. ENGLE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,310,492 Nagelvoort Feb. 9, 1943 2,364,090 Nagelvoort Dec. 5, 1944 2,379,389 Tillotson June 26, 1945 2,382,731 Little Aug. 14, 1945
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US640676A US2461551A (en) | 1946-01-11 | 1946-01-11 | Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US640676A US2461551A (en) | 1946-01-11 | 1946-01-11 | Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2461551A true US2461551A (en) | 1949-02-15 |
Family
ID=24569250
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US640676A Expired - Lifetime US2461551A (en) | 1946-01-11 | 1946-01-11 | Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2461551A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582160A (en) * | 1948-10-20 | 1952-01-08 | Interchem Corp | Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal |
| US2582139A (en) * | 1949-07-08 | 1952-01-08 | Interchem Corp | Resinous products of the reaction of styrene with resins derived from bituminous coals of utah |
| US2673845A (en) * | 1951-10-10 | 1954-03-30 | Armstrong Cork Co | Trowelable synthetic rubber adhesives |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2310492A (en) * | 1940-12-05 | 1943-02-09 | Nagelvoort Adriaan | Recovering resins from coal |
| US2364090A (en) * | 1942-02-23 | 1944-12-05 | Nagelvoort Adrlaan | Purifying resins |
| US2379389A (en) * | 1942-12-14 | 1945-06-26 | Neil E Tillotson | Rubber or rubberlike composition and method |
| US2382731A (en) * | 1942-09-26 | 1945-08-14 | Hercules Powder Co Ltd | Adhesive |
-
1946
- 1946-01-11 US US640676A patent/US2461551A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2310492A (en) * | 1940-12-05 | 1943-02-09 | Nagelvoort Adriaan | Recovering resins from coal |
| US2364090A (en) * | 1942-02-23 | 1944-12-05 | Nagelvoort Adrlaan | Purifying resins |
| US2382731A (en) * | 1942-09-26 | 1945-08-14 | Hercules Powder Co Ltd | Adhesive |
| US2379389A (en) * | 1942-12-14 | 1945-06-26 | Neil E Tillotson | Rubber or rubberlike composition and method |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2582160A (en) * | 1948-10-20 | 1952-01-08 | Interchem Corp | Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal |
| US2582139A (en) * | 1949-07-08 | 1952-01-08 | Interchem Corp | Resinous products of the reaction of styrene with resins derived from bituminous coals of utah |
| US2673845A (en) * | 1951-10-10 | 1954-03-30 | Armstrong Cork Co | Trowelable synthetic rubber adhesives |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0192930B1 (en) | Natural rubber containing compositions with increased tear strength | |
| US3519585A (en) | Pressure sensitive adhesive composition | |
| US3714110A (en) | Oil extended polyurethanes based on hydroxy terminated diene polymers | |
| US2638460A (en) | Butadiene polymers as elastomer additives | |
| JP3175016B2 (en) | High hardness rubber composition | |
| EP0020501A4 (en) | Polymer compositions and a method for enhancement in phase compatibility of elastomers with relatively rigid polymers. | |
| US2461551A (en) | Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal | |
| US2582264A (en) | Softening agent for rubber and resulatant rubber composition | |
| CA1128248A (en) | Elastomers with improved metal adhesion | |
| US2382731A (en) | Adhesive | |
| US2421627A (en) | Rubberlike substances and compounding material | |
| US2638456A (en) | Plastic compound containing synthetic rubber and anthracite coal | |
| US3238164A (en) | Tall oil pitch-c1-c18 monohydric alcohol compositions and use thereof in rubber | |
| US2440299A (en) | Method of compounding rubbery materials | |
| US2550363A (en) | Lactam plasticizer for rubbers | |
| US2582160A (en) | Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal | |
| US3243390A (en) | Water-base paint containing hydrogenated hydrocarbon resin and butyl rubber | |
| DE1073735B (en) | Vulcanization of butyl rubber | |
| US2537908A (en) | Compounded rubber stock | |
| US2461553A (en) | Adhesive composition containing polychloroprene rubber and a resin occurring in utahresinbearing coal | |
| US2427942A (en) | Vulcanization of butadiene-styrene copolymer | |
| US2340699A (en) | Synthetic rubber composition | |
| US2330698A (en) | Plastic composition | |
| US2794006A (en) | Pan process of reclaiming rubber | |
| US3231546A (en) | Solid styrene-sulfur compounds and vulcanizates made therewith |